HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 2-Isopropoxy-5-(3-methylpiperidinosulfonyl)benzoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Methylpiperidine | HCID 79081 | — |
| Reactant | 2-Fluoro-5-chlorosulfonylbenzoic acid | HCID 608984 | — |
| Reactant | 2-Fluoro-5-(3-methylpiperidinosulfonyl)benzoic acid | HCID 3651116 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-Isopropoxy-5-(3-methylpiperidinosulfonyl)benzoic Acid | HCID 20505978 | — |
Reaction Steps
2-Fluoro-5-chlorosulfonylbenzoic acid is heated with 3-methylpiperidine by the method of Example 1, and the resulting 2-fluoro-5-(3-methylpiperidinosulfonyl)benzoic acid (5 millimoles) is heated on a steam bath for 31/2 hours in isopropyl alcohol (50 ml.) with 5 millimoles of sodium hydride (56.6% suspension in mineral oil). The reaction mixture is evaporated to dryness, and then dissolved in 50 ml. of water. After washing with ether, the aqueous solution is acidified with concentrated HCl. The acid solution is then extracted with ether, and the ether extract washed with water and evaporated to an oil. The oil crystallizes from isopropyl ether-hexane. Recrystallization from the same solvent mixture affords the product, m.p. 102°-104° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04377521 |
| Source dataset | uspto-grants-1983_03 |
| ORD ID | ord-37727aec56bf4f1e9f7467325a85ee59 |
| Source note | uspto-grants-1983_03 |